1986
DOI: 10.1038/321446a0
|View full text |Cite
|
Sign up to set email alerts
|

Expression of biologically active viral satellite RNA from the nuclear genome of transformed plants

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
126
0
2

Year Published

1987
1987
2007
2007

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 243 publications
(128 citation statements)
references
References 22 publications
0
126
0
2
Order By: Relevance
“…However, this approach may involve environmental hazards (Nelson et al, 1988) which could be eliminated through the expression of disabled forms of satellite RNA that cannot be acquired and transmitted by CMV (Baulcombe et al, 1986) and in which sequences affecting symptom production have been deleted or modified. It is not yet known to what extent At05/188 or A109/191 fit those requirements.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…However, this approach may involve environmental hazards (Nelson et al, 1988) which could be eliminated through the expression of disabled forms of satellite RNA that cannot be acquired and transmitted by CMV (Baulcombe et al, 1986) and in which sequences affecting symptom production have been deleted or modified. It is not yet known to what extent At05/188 or A109/191 fit those requirements.…”
Section: Discussionmentioning
confidence: 99%
“…The accession received was designated I 17N' satellite RNA in order to distinguish it from the I17N satellite RNA described by Jacquemond & Lauquin (1988) (see Results section). Satellite eDNA clones were described previously in Devic et al (1989) (Y satellite RNA) and Baulcombe et al (1986) (I17N" satellite RNA). The inocula of CMV-KIN and TAV used as helper viruses were extracts of total nucleic acids from infected plants that were prepared as described by Devic et al (1989).…”
Section: Methodsmentioning
confidence: 99%
“…Into the Bam HI site of the expression cassette pRokl [3] we cloned the hygromycin phosphotransferase (HPTII) gene (a 1 kb Barn HI fragment with a single ATG to improve the translation efficiency; van den Elzen, unpublished) and modified the resulting plasmid by filling in the Bam HI site between the HPTII gene and the nopaline synthase (nos) polyadenylation signal. After the cloning of plasmid pUC18, containing the bases 2640 (SphI)-6130(XhoI) from the T-DNA of pTiAch5 [ 12] in the Hind III site, the plasmid has been renamed pTT218 ( Fig.…”
Section: Phenotypic Assay Vectors For Tam3 and Acmentioning
confidence: 99%
“…The vector was constructed in two steps. First, a I kb BamHI fragment containing HPT II was inserted into the BamHI site of the expression cassette pRoM (Baulcombe et al 1986). After filling-in the BamHI site between HPT II and the polyadenylation signal, the resulting plasmid was named pTT212.…”
Section: Methodsmentioning
confidence: 99%